Official git repository for Biopython (originally converted from CVS)
- python
- bioinformatics
- genomics
- biopython
47,133 repositories indexed
1–24 of 45 · Most stars
Official git repository for Biopython (originally converted from CVS)
Official repository for the Boltz biomolecular interaction models
Deep probabilistic analysis of single-cell and spatial omics data
ProtTrans is providing state of the art pretrained language models for proteins. ProtTrans was trained on thousands of GPUs from Summit and hundreds of Google TPUs using Transformers Models.
A Deep Learning Toolkit for DTI, Drug Property, PPI, DDI, Protein Function Prediction (Bioinformatics)
🦖 ClawBio - The first bioinformatics-native AI agent skill library. Local-first. Reproducible. Open. Free.
Scientific workflow engine designed for simplicity & scalability. Trivially transition between one off use cases to massive scale production environments
ADAM is a genomics analysis platform with specialized file formats built using Apache Avro, Apache Spark, and Apache Parquet. Apache 2 licensed.
Validated, scalable, community developed variant calling, RNA-seq and small RNA analysis
Official implementation for HyenaDNA, a long-range genomic foundation model built with Hyena
C++ library and cmdline tools for parsing and manipulating VCF files with python and zig bindings
Fast, sensitive and accurate integration of single-cell data with Harmony
Lightweight, super fast C/C++ (& Python) library for sequence alignment using edit (Levenshtein) distance.
Generative biopolymer design with rich conditioning.
[ICLR 2024] DNABERT-2: Efficient Foundation Model and Benchmark for Multi-Species Genome
RNA Velocity generalized through dynamical modeling
Official repository for the ProteinGym benchmarks
A Practical and Efficient NCBI Taxonomy Toolkit, also supports creating NCBI-style taxdump files for custom taxonomies like GTDB/ICTV
Sequential regulatory activity predictions with deep convolutional neural networks.
A dependency-free cross-platform swiss army knife for PDB files.
Native R and Python sample-deletion robustness for omics: candidate certificates, minimum deletion bounds, Bioconductor model refits and donor-level pseudobulk
RNA-seq prediction with deep convolutional neural networks.
Schema and generated objects for biolink data model and upper ontology
talk with NCBI entrez using R